510(k) Report

FDA applicant

Nordan Smith Welding Supplies

Hattiesburg, MS3 decisions1994–19950 recalls

FDA records 3 decisions for Nordan Smith Welding Supplies (Hattiesburg, MS) from 1994 to 1995: 3 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and BXK (Gas, Calibration (Specified Concentration)). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

How often FDA has decided Nordan Smith Welding Supplies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nordan Smith Welding Supplies since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nordan Smith Welding Supplies by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Nordan Smith Welding Supplies’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • GEXPowered Laser Surgical Instrument1decision
  • BXKGas, Calibration (Specified Concentration)1decision
  • BZCCalculator, Pulmonary Function Data1decision

What has FDA decided for it lately?

  • K942864Lung DiffusionNordan Smith Welding Supplies · 1995
  • K942866Clinical Blood Gas MixtureNordan Smith Welding Supplies · 1994
  • K942865Laser Gas MixtureNordan Smith Welding Supplies · 1994

All 3 as Nordan Smith Welding Supplies →